K-number	K060047
Device name	CARTO RMT EP NAVIGATION SYSTEM V8
Applicant	Biosense Webster, Inc.
Product code	DRF
Device class	Class II
Decision date	Jun 19, 2006
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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CARTO RMT EP NAVIGATION SYSTEM V8

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